Enantiospecific Alkynylation of Alkylboronic Esters. - Wikidata - wikimedia - TriplyDB

Enantiospecific Alkynylation of Alkylboronic Esters.

Enantiospecific Alkynylation of Alkylboronic Esters.

http://www.wikidata.org/entity/Q39397811

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Stereospecific functionalizations and transformations of secondary and tertiary boronic esters.Short Enantioselective Total Synthesis of Tatanan A and 3-epi-Tatanan A Using Assembly-Line Synthesis.Enantiospecific Trifluoromethyl-Radical-Induced Three-Component Coupling of Boronic Esters with Furans.Enantioselective γ-borylation of unsaturated amides and stereoretentive Suzuki-Miyaura cross-coupling.Selective uni- and bidirectional homologation of diborylmethane.A general, modular method for the catalytic asymmetric synthesis of alkylboronate esters.Iterative assembly line synthesis of polypropionates with full stereocontrol.Stereocontrolled Synthesis of Polypropionate Fragments based on a Building Block Assembly Strategy using Lithiation-Borylation Methodologies.Pd-Catalyzed Conjunctive Cross-Coupling between Grignard-Derived Boron "Ate" Complexes and C(sp2) Halides or Triflates: NaOTf as a Grignard Activator and Halide Scavenger.Transition-metal-free synthesis of 1,1-diboronate esters with a fully substituted benzylic center via diborylation of lithiated carbamates.

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Enantiospecific Alkynylation of Alkylboronic Esters.

http://www.wikidata.org/entity/Q39397811

description

2016 nî lūn-bûn

@nan

2016年の論文

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2016年論文

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2016年論文

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2016年論文

@zh-hk

2016年論文

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2016年論文

@zh-tw

2016年论文

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2016年论文

@zh

2016年论文

@zh-cn

name

Enantiospecific Alkynylation of Alkylboronic Esters.

@en

Enantiospecific Alkynylation of Alkylboronic Esters.

@nl

type

label

Enantiospecific Alkynylation of Alkylboronic Esters.

@en

Enantiospecific Alkynylation of Alkylboronic Esters.

@nl

prefLabel

Enantiospecific Alkynylation of Alkylboronic Esters.

@en

Enantiospecific Alkynylation of Alkylboronic Esters.

@nl

P1433

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P1433

Angewandte Chemie International Edition

P1476

Enantiospecific Alkynylation of Alkylboronic Esters.

@en

P2093

Eddie L Myers

http://www.w3.org/2001/XMLSchema#string

P2860

A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes

A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)

An Improved One-pot Procedure for the Synthesis of Alkynes from Aldehydes

Polyketide assembly by alkene-alkyne reductive cross-coupling: spiroketals through the union of homoallylic alcohols

The discovery of novel reactivity in the development of C-C bond-forming reactions: in situ generation of zinc acetylides with Zn(II)/R(3)N.

Cu-catalyzed azide-alkyne cycloaddition

Cu-catalyzed Fe-driven C(sp)-C(sp) and C(s)p-C(sp2) cross-coupling: an access to 1,3-diynes and 1,3-enynes.

Transition-metal-catalyzed addition of heteroatom-hydrogen bonds to alkynes.

Lithium diisopropylamide: solution kinetics and implications for organic synthesis.

The Enantioselective Addition of Alkyne Nucleophiles to Carbonyl Groups.

P304

4270-4274

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scholarly article

P356

10.1002/ANIE.201600599

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P433

13

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55

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Varinder Aggarwal

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2016-03-02T00:00:00Z

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26934427

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4804747

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